Ontology highlight
ABSTRACT: Background
Assays of multiple tumor samples frequently reveal recurrent genomic aberrations, including point mutations and copy-number alterations, that affect individual genes. Analyses that extend beyond single genes are often restricted to examining pathways, interactions and functional modules that are already known.Methods
We present a method that identifies functional modules without any information other than patterns of recurrent and mutually exclusive aberrations (RME patterns) that arise due to positive selection for key cancer phenotypes. Our algorithm efficiently constructs and searches networks of potential interactions and identifies significant modules (RME modules) by using the algorithmic significance test.Results
We apply the method to the TCGA col
SUBMITTER: Miller CA
PROVIDER: S-EPMC3102606 | biostudies-literature | 2011 Apr
REPOSITORIES: biostudies-literature